# Bimatoprost

NDC: 0781-6206
Generic name: Bimatoprost
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20161206

FDA application: ANDA202719

## Active ingredients

- BIMATOPROST: .3 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-6206"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-6206
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=27bef7e1-750a-4ac1-ab5f-e4c0121ffcbc